drugset / Trial / NCT00227370

Comparison of Oral Valganciclovir and Placebo for the Prevention of Cytomegalovirus (CMV) After Lung Transplantation

NCT00227370

Phase 3 Completed 136 enrolled Duke University Roche Pharma AG · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

The study evaluated the efficacy and safety of a prolonged, continuous course of Valganciclovir (Valgan) in the prevention of CMV by comparing 3 months of Vaglanciclovir, the standard of care upon initiation of the study, to 12 months of Valganciclovir.

Timeline

Start
2003-07
Primary completion
2008-04
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Valganciclovir Small molecule 900 mg Oral